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rs9499708

From SNPedia

Orientationplus
Stabilizedplus
Make rs9499708(C;C)
Make rs9499708(C;T)
Make rs9499708(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position103997492
is asnp
is mentioned by
dbSNPrs9499708
dbSNP (classic)rs9499708
ClinGenrs9499708
ebirs9499708
HLIrs9499708
Exacrs9499708
Gnomadrs9499708
Varsomers9499708
LitVarrs9499708
Maprs9499708
PheGenIrs9499708
Biobankrs9499708
1000 genomesrs9499708
hgdprs9499708
ensemblrs9499708
geneviewrs9499708
scholarrs9499708
googlers9499708
pharmgkbrs9499708
gwascentralrs9499708
openSNPrs9499708
23andMers9499708
SNPshotrs9499708
SNPdbers9499708
MSV3drs9499708
GWAS Ctlgrs9499708
GMAF0.258
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22889921OA-icon.png]
Trait Obsessive-compulsive disorder
Title Genome-wide association study of obsessive-compulsive disorder.
Risk Allele
P-val 3E-6
Odds Ratio 1.20 NR